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Getting MAD at MYC
Torchia and Ashwell express commentary on the study by Li et al identify a molecular mechanism for the regulation of c-MYC expression and function and describe a small molecule that inhibits MYC by enhancing the expression of a functional MYC antagonist in the transcriptional regulatory network. The...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2018-10, Vol.115 (40), p.9821-9823 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Torchia, Maria Letizia Giardino Ashwell, Jonathan D. |
description | Torchia and Ashwell express commentary on the study by Li et al identify a molecular mechanism for the regulation of c-MYC expression and function and describe a small molecule that inhibits MYC by enhancing the expression of a functional MYC antagonist in the transcriptional regulatory network. The study uses the functional interplay between cIAP1 and MAD1 as a starting point to develop reagents that reverse the cell growth-promoting effects of MYC. MYC protooncogene family (MYC, MYCN, and MYCL), known variously as super, master, or global transcription factors, affects the expression of an estimated 15% of the entire genome, which may in fact be an underestimate, given that Myc accumulates not just at specific DNA target sites but also in the promoter regions of most actively transcribed genes and leads to their amplification. |
doi_str_mv | 10.1073/pnas.1813867115 |
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subjects | Adenine Nucleotides Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Basic-Leucine Zipper Transcription Factors Biological Sciences c-Myc protein Commentaries COMMENTARY Deoxyribonucleic acid DNA DNA-Binding Proteins Gene expression Genomes Molecular biology Myc protein Mycophenolic Acid - analogs & derivatives Proto-Oncogene Proteins c-myc Reagents Repressor Proteins Transcription Factors |
title | Getting MAD at MYC |
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